FDA Inspection
Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited)Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited) – FDA Inspection, May 8, 2026
Record Details
This FDA Inspection record concerns Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited), with an inspection on May 8, 2026, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- May 8, 2026
- Product Type
- Human Drugs
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ID · 92270659-ee38-403e-b67f-83423447fc11
Inspection Facts
- Inspection number
- 1321654
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited)
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 4, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 1, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 12, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 20, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited)
- FDA Inspection 1086346 - 2019-03-04
- FDA Inspection 921990 - 2015-04-01
- FDA Inspection 829337 - 2013-04-12
- FDA Inspection 635196 - 2009-11-20
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